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Kanumuri Siva Rama Raju

Researcher at Central Drug Research Institute

Publications -  43
Citations -  951

Kanumuri Siva Rama Raju is an academic researcher from Central Drug Research Institute. The author has contributed to research in topics: Bioavailability & Pharmacokinetics. The author has an hindex of 17, co-authored 41 publications receiving 751 citations. Previous affiliations of Kanumuri Siva Rama Raju include Academy of Scientific and Innovative Research.

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Comparative assessment of bioanalytical method validation guidelines for pharmaceutical industry

TL;DR: The present review highlights the variations, similarities and comparison between bioanalytical method validation guidelines issued by major regulatory authorities worldwide.
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Synthesis and Insight into the Structure–Activity Relationships of Chalcones as Antimalarial Agents

TL;DR: Licochalcone A (I), isolated from the roots of Chinese licorice, is the most promising antimalarial compound reported so far and two similar chalcones, medicagenin (II) and munchiwarin (III), from Crotalaria medicagenia, which exhibitedAntimalarial activity against Plasmodium falciparum .
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Pharmacokinetics study of arteether loaded solid lipid nanoparticles: An improved oral bioavailability in rats

TL;DR: From the results, it can be concluded that ART-SLN offers a new approach to improve the oral bioavailability of ART and may help to protect the acid degradation of ART in stomach.
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Antileishmanial Activity of Pyrazolopyridine Derivatives and Their Potential as an Adjunct Therapy with Miltefosine.

TL;DR: Investigating the effect of 6j on Leishmania promastigotes revealed that it induced molecular events, such as a loss in mitochondrial membrane potential, externalization of phosphatidylserine, and DNA fragmentation, that ultimately resulted in the programmed cell death of the parasite.
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Naturally Occurring Carbazole Alkaloids from Murraya koenigii as Potential Antidiabetic Agents.

TL;DR: Koenidine (4) was identified as a metabolically stable antidiabetic compound, when evaluated in a rodent type 2 model, and showed a considerable reduction in the postprandial blood glucose profile with an improvement in insulin sensitivity.